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Pleosporales - CBS - KNAW

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Fungal Diversity<br />

(<strong>CBS</strong> 627.86) was isolated by K. & L. Holm, who had<br />

examined the type specimen of L. nucula (Holm and Holm<br />

1988), the culture of Lophiostoma macrostomum used in<br />

the analysis are unverified (see comment by Zhang et al.<br />

2009b). For the purpose of this monograph we tentatively<br />

maintain Lophiotrema as distinct from Lophiostoma.<br />

Macroventuria Aa, Persoonia 6: 359 (1971).<br />

(Didymellaceae)<br />

Generic description<br />

Habitat terrestrial, saprobic. Ascomata small, solitary, scattered,<br />

or in groups, initially immersed, becoming erumpent, to nearly<br />

superficial, globose to subglobose, roughened with cylindrical<br />

setae erect from apex. Peridium thin, membranous. Hamathecium<br />

of cellular pseudoparaphyses, seems to easily disappear<br />

when mature. Asci bitunicate, somewhat obclavate to fusoid.<br />

Ascospores fusoid with broadly to narrowly rounded ends,<br />

hyaline, 1-septate, constricted at the septum.<br />

Anamorphs reported for genus: none.<br />

Literature: van der Aa 1971; von Arx and Müller 1975;<br />

Barr 1987a.<br />

Type species<br />

Macroventuria wentii Aa, Persoonia 6: 361 (1971). (Fig. 53)<br />

Ascomata 135–180 μm diam., rarely more than 200 μm<br />

diam., solitary, scattered or in groups, initially immersed,<br />

becoming erumpent, to nearly superficial, with basal wall<br />

remaining immersed in host tissue, globose to subglobose,<br />

broadly or narrowly conical, setae erect from the apical region of<br />

the ascomata, cylindrical or tapering to the rounded or pointed<br />

tip, brown, up to 90 μm long, 5–7.5 μm thick (Fig. 53a).<br />

Peridium, 25–35 μm thick, 2-layered, out layer composed of<br />

relatively thick-walled cells of textura angularis, cell wall up to<br />

3 μm thick; inner layer cells with a thinner wall and subhyaline;<br />

near apex cells smaller (Fig. 53a). Hamathecium of cellular<br />

pseudoparaphyses, 1–2 μm thick, evanescing not sure. Asci 75–<br />

93×24–30 μm, 8-spored, without pedicel, bitunicate, somewhat<br />

obclavate to fusoid (Fig. 53b). Ascospores 22–32×8–14 μm, 1–<br />

3 seriate, fusoid with broadly to narrowly rounded ends, hyaline,<br />

1-septate, constricted at the septum, smooth (Fig. 53b) (description<br />

adapted from van der Aa 1971).<br />

Anamorph: none reported.<br />

Material referred: USA, Nevada; Death Valley, plant<br />

litter, F.W. Went, 229, 1970 (<strong>CBS</strong> 526.71, holotype).<br />

Notes<br />

Morphology<br />

Macroventuria was formally established by van der Aa<br />

(1971) represented by M. anomochaeta and M. wentii based<br />

on its “near-hyaline, 1-septate ascospores, setose ascomata,<br />

and saprobic life style”. Almost all of the above characters<br />

(except the saprobic life style) point this group of fungi to<br />

Venturiaceae. Thus Macroventuria was assigned to this<br />

family as a relatively primitive genus (van der Aa 1971).<br />

Subsequently, von Arx and Müller (1975) assigned Macroventuria<br />

to Pseudosphaeriaceae (Dothideales), and this<br />

proposal was followed by Barr (1987a).<br />

Phylogenetic study<br />

Phylogenetic analysis based on combined SSU rDNA<br />

and LSU rDNA sequences indicated that both of Macroventuria<br />

anomochaeta and M. wentii form a robust clade<br />

with Leptosphaerulina argentinensis (Speg.) J.H. Graham<br />

& Luttr., L. australis, L. trifolii (Rostr.) Petr. and<br />

Platychora ulmi, which appear to share phylogenetic<br />

affinities with the Leptosphaeriaceae and Phaeosphaeriaceae,<br />

but detached from other members of Venturiaceae<br />

and Pleosporaceae (Kodsueb et al. 2006a). In addition,<br />

culture characters also support the close relationship<br />

between Macroventuria and Leptosphaerulina (Barr<br />

1987a). Analysis based on five genes, i.e. SSU, LSU,<br />

RPB1, RPB2 andTEF1, indicated Macroventuria anomochaeta<br />

resides in the well supported clade of Didymellaceae<br />

(Zhang et al. 2009a).<br />

Concluding remarks<br />

The morphological characters, such as small ascomata<br />

and hyaline, 1-septate ascospores all point at Didymellaceae,<br />

thus the familial status of Macroventuria is verified.<br />

Mamillisphaeria K.D. Hyde, S.W. Wong & E.B.G. Jones,<br />

Nova Hedwigia 62: 514 (1996b). (?Melanommataceae)<br />

Generic description<br />

Habitat freshwater, saprobic. Ascomata superficial, scattered<br />

or gregarious, conical, carbonaceous, papillate.<br />

Hamathecium of dense, filliform, trabeculate pseudoparaphyses.<br />

Asci broadly clavate to clavate, with small ocular<br />

chambers and short pedicels. Ascospores of two types, (1):<br />

2-4-seriate, ellipsoid, hyaline, slightly constricted at the<br />

main septum; with apical appendages at each end and<br />

around the ascospore; (2) 1-2-seriate, ellipsoid to fusoid,<br />

brown, with mucilaginous sheath around the ascospore<br />

(Hyde et al. 1996b).<br />

Anamorphs reported for genus: none.<br />

Literature: Hyde et al. 1996a, b.<br />

Type species<br />

Mamillisphaeria dimorphospora K.D. Hyde, S.W. Wong<br />

& E.B.G. Jones, Nova Hedwigia 62: 515 (1996b). (Fig. 54)

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